Research Area
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Description
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Hyperlipidaemia ,Type-2 diabetes mellitus |
Biological Activity
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Description
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GSK-1292263 is a novel GPR119 agonist. |
Targets
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GPR119 |
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IC50 |
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In Vitro
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GSK-1292263 is selected from 1538 compounds by using Hypo1, the Fit-Value and Estimate of GSK-1292263 that is aligned in Hypo1 are 8.8 and 7.7 (nM), respectively. [1] |
In Vivo
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GSK-1292263 administrated at a single dose of 3-30 mg/kg in the absence of nutrients correlates with increased levels of circulating gastrointestinal peptides, including glucagon-like peptide 1 (GLP-1), gastric inhibitory polypeptide (GIP), peptide YY (PYY) and glucagon in male Sprague-Dawley rats, the increase is enhanced following administration of glucose in the oral glucose tolerance test (OGTT). GSK-129226 significant increases in the peak insulin response and insulin AUC(0-15 min) of 30-60% compared with values in the vehicle control cohort in the intravenous glucose tolerance test in rats, this insulin upregulation correlated with a significant increase in the glucose disposal rate. GSK-1292263 is associated with a statistically significant increase in insulin immunoreactivity in pancreatic sections in a 6-week study performed in Zucker diabetic fatty rats, compared with insulin immunoreactivity in samples obtained from rats receiving vehicle control. GSK-1292263 administrated at dose of 10 or 30 mg/kg or vehicle control at 2 hours prior to insulin infusion in hyperinsulinemic-euglycemic clamps stimulates glucagon secretion without increasing blood glucose levels Sprague-Dawley rats. [2] |
Clinical Trials
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GSK1292263 has finished Phase II clinical trial for Diabetes Mellitus, Type 2. |
Features
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Protocol
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Animal Study
[2]
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Animal Models |
male Sprague-Dawley rats |
Formulation |
0.9% sodium chloride solution |
Doses |
3-30 mg/kg |
Administration |
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